| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135344005-135344227 | Common:1; Rare:40 | ||||
| chrX:135344608-135344863 | Common:1; Rare:51 | ||||
| chrX:135973657-135973872 | Rare:70 | ||||
| chrX:135985347-135985525 | Rare:53; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chrX:136497107-136497420 | Common:3; Rare:81 | ||||
| chrX:136880595-136880901 | Common:1; Rare:71 | ||||
| chrX:138711199-138711494 | Common:2; Rare:71 | ||||
| chrX:138711638-138711925 | Common:2; Rare:53 | ||||
| chrX:139832179-139832370 | Rare:36 | ||||
| chrX:139933000-139933260 | Rare:47 | ||||
| chrX:141177030-141177325 | Common:1; Rare:45 | ||||
| chrX:143634492-143634607 | Rare:25 | ||||
| chrX:147911776-147912191 | Common:3; Rare:125 | ||||
| chrX:149540905-149541094 | Common:3; Rare:35 | ||||
| chrX:149631713-149631863 | Common:1; Rare:50 |